CAS: 128249-70-7; 2,6-Bis((R)-4-Phenyl-4,5-Dihydrooxazol-2-yl)Pyridine

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CAS号3739-94-4 2,6-吡啶二甲酰氯 | CAS号56613-80-0 D-苯甘氨醇 | CAS号661464-60-4 N,N'-bis[(1R)-2... | CAS号5431-44-7 2,6-吡啶二甲醛 | CAS号5453-67-8 2,6-吡啶二甲酸二甲酯 | CAS号499-83-2 2,6-吡啶二羧酸

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    吡啶-2.6-二羧酸二甲酯置于三乙胺,对甲苯磺酰氯体系中,用 二氯甲烷 用作溶剂,化学反应 36.0H,反应生成2,6-二[(4R)-4-苯基-2-恶唑啉基]吡啶
    参考文献:Asymmetric Catalysis In A Micro Reactor-ce,Yb And Lu Catalysed Enantioselective Addition Of Trimethylsilyl Cyanide To Benzaldehyde
    标题:Asymmetric Catalysis In A Micro Reactor-ce,Yb And Lu Catalysed Enantioselective Addition Of Trimethylsilyl Cyanide To Benzaldehyde
    摘要:A T-Shaped Micro Reactor Was Used For The Optimisation Of Reaction Conditions For The Enantioselective Silyleyanation Of Benzaldehyde Catalysed By Lanthanide-Pybox Complexes. Compared To A Conventional Batch Procedure,Higher Conversion Was Observed Within Shorter Reaction Time. The Micro Reactor Process Involving Lu(III) Afforded Essentially The Same Enantioselectivity As The Batch Process (73 Vs 76% Ee),Whereas The Enantioselectivity Was Lower In The Micro Reactor For Catalysts Containing Yb(III) (53 Compared To 72%). Ce(III) Provided Very Low Selectivity In Both Types Of Processes (1 And 11 % Ee,Respectively). A Study Of The Effect Of Additives Showed That The Enantioselectivity In The Yb Catalysed Reaction Performed In The Micro Reactor Could Be Increased To 66%,Whereas Only A Minor Improvement,To 78% Ee,Was Observed In The Reaction With Lu. (C) 2004 Elsevier Ltd. All Rights Reserved.
    Doi:10.1016/j.Tet.2004.08.080

    海关参考信息

    专利信息


    专利号:US-11926589-B2
    优先权日:2019-07-09
    标 题 :Process for the synthesis of non-racemic cyclohexenes
    发明人:REISMAN SARAH; ROMBOLA MICHAEL; LADD CAROLYN L; MCLAUGHLIN MARTIN JOHN; ZUEND STEPHAN; GOETZ ROLAND
    权利人:BASF CORP; CALIFORNIA INST OF TECHN
    摘要:This invention relates to a process for the synthesis of a non-racemic cyclohexene compound of formula (I) by a Diels-Alder reaction of a compound of formula (II) with a compound of formula (III) wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and Y have the meanings as defined in the description in the presence of a catalyst comprising at least one m-valent metal cation M m+ wherein the metal M is selected from Scandium (Sc), Yttrium (Y), Lanthanum (La), Cerium (Ce), Praseodymium (Pr), Neodymium (Nd), Promethium (Pm), Samarium (Sm), Europium (Eu), Gadolinium 15 (Gd), Terbium (Tb), Dysprosium (Dy), Holmium (Ho), Erbium (Er), Thulium (Tm), Ytterbium (Yb), Lutetium (Lu), Gallium (Ga) and Indium (In), and m is an integer of 1, 2 or 3, and a chiral ligand of the formula (IV) wherein R 10a , R 10b , R 10c , R 10d , R 10a′ , R 10b′ , R 10c′ , R 10d′ , Z and Z′ have the meanings as defined in the description.

    专利号:US-8431745-B2
    优先权日:2006-03-29
    标题 :Process for preparation of HIV protease inhibitors
    发明人:CRAWFORD KENNETH R; DOWDY ERIC D; GUTIERREZ ARNOLD; POLNIASZEK RICHARD P; YU RICHARD HUNG CHIU
    权利人:CRAWFORD KENNETH R; DOWDY ERIC D; GUTIERREZ ARNOLD; POLNIASZEK RICHARD P; YU RICHARD HUNG CHIU; GILEAD SCIENCES INC
    摘要:A process for the synthesis of bisfuran intermediates useful for preparing antiviral HIV protease inhibitor compounds is hereby disclosed.

    专利号:WO-2021007141-A1
    优先权日:2019-07-09
    标 题 :Process for the synthesis of non-racemic cyclohexenes

    专利号:US-2022267247-A1
    优先权日:2019-07-09
    标题:Process for the synthesis of non-racemic cyclohexenes

    专利号:US-11459287-B1
    优先权日:2021-10-06
    标题 :Arene-immobilized ru(II)TsDPEN complexes: synthesis and applications to the asymetric transfer hydrogenation of ketones
    发明人:ALSHAIKH HIND FAISAL; KNIGHT JULIAN
    权利人:UNIV KING ABDULAZIZ
    摘要:Arene-immobilized Ru(II)TsDPEN Noyori-Ikariya catalysts anchored to silica through the coordinated η6-arene are provided. The catalysts efficiently catalyze many reactions, including the asymmetric transfer hydrogenation of ketones to alcohols.

    专利号:EP-3997082-A1
    优先权日:2019-07-09
    标 题 :Process for the synthesis of non-racemic cyclohexenes
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    主要参考文献

    参考标题:Synthesis Of Copper(I) Complexes Containing Enantiopure Pybox Ligands. First Assays On Enantioselective Synthesis Of Propargylamines Catalyzed By Isolated Copper(I) Complexes
    作者:María Panera,Josefina Díez,Isabel Merino,Eduardo Rubio,M. Pilar Gamasa |发布日期:2009.12.7
    摘要:State And Confirm That These Ionic Compounds Exist In Solution As Stable, Discrete, Cationic Complexes. The Complexes 1−4, 6, 9, 10, And 16 As Well As The Previously Reported [cu2(S,S)-Ipr-Pybox}2][otf]2 Have Been Assayed As Catalysts In The Enantioselective Synthesis Of Propargylamines. The Dinuclear Complexes [cu2(R,R)-Ph-Pybox}2][x]2 (2, 4) Were Found To Be The Most Efficient Catalysts (Up To 89%

    合成参考文献


    摘要:Li, W.; Liu, X. H.; Feng, X. M., Science of Synthesis Knowledge Updates, (2021) 1, 27.
    摘要:Wu, X.-F., Science of Synthesis Knowledge Updates, (2014) 1, 328.
    摘要:Atodiresei, I.; Rueping, M., Science of Synthesis Knowledge Updates, (2017) 1, 387.
    摘要:Ipaktschi, J.; Saidi, M. R., Science of Synthesis Knowledge Updates, (2012) 4, 429.
    摘要:Liu, Z.-Q., Science of Synthesis, (2020) , 361.
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